List of variants in gene KIT reported as likely benign for immune system cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000222.3(KIT):c.2502G>A (p.Lys834=)	rs146992614	0.00014
NM_000222.3(KIT):c.840G>C (p.Ala280=)	rs142772432	0.00004
NM_000222.3(KIT):c.531C>T (p.Arg177=)	rs756722358	0.00001

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